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Hybrid Event, 20 - 24 June 2022
In-Person: Dublin, IrelandDigital Experience: One track will be live-streamed
each day in GMT time zone, with on-demand recording access for all other tracks
made available on the afternoon of the following day. Learn more on the Digital
Experience page.
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Hybrid Event, 20 - 24 June 2022
In-Person: Dublin, IrelandDigital Experience: One track will be live-streamed
each day in GMT time zone, with on-demand recording access for all other tracks
made available on the afternoon of the following day. Learn more on the Digital
Experience page.


Hybrid Event, 20 - 24 June 2022
In-Person: Dublin, Ireland,
Digital Experience: One track will be live-streamed each day in GMT time zone,
with on-demand recording access for all other tracks made available on the
afternoon of the following day. Learn more on the Digital Experience page.


ISO 10993: STAY AHEAD OF THE LATEST REVISIONS AND BEST PRACTICE


BIOCOMPATIBILITY TESTING AND EVALUATIONS REQUIREMENTS: FEEDBACK FROM TC 194
WORKING GROUP, COMPETENT AUTHORITY, NOTIFIED BODY AND INDUSTRY EXPERTS

Including ISO 10993-1 updates, part 17 insights, part 23 applications,
implementation timelines, risk assessments, chemical characterisation,
extractables and leachables, and more!
See The Biocompatibility Agenda



IMPLEMENT BIOLOGICAL EVALUATION PLANS FOR YOUR MEDICAL DEVICES WITH CONFIDENCE




ISO 10993 UPDATES AND GUIDANCE

 * How will the recent part 1 revision impact your biocompatibility testing,
   evaluations and risk assessments? Ensure you’re prepared with expert guidance
 * Practical advice for applying part 18 for chemical characterisation of
   extractables and leachables, analytical techniques, and common pitfalls
 * Get to grips with the recent part 17 updates for the establishment of
   allowable limits for leachable substances
 * Experiences with adapting to the complexities of the new part 23 standard for
   irritation testing


ADDRESS YOUR BIOCOMPATIBILITY QUESTIONS IN INTERACTIVE PANEL DISCUSSIONS

 * What is the future of in vitro testing? Leading perspectives on what’s
   possible and insights on acceptance of ISO 10993-23, tests for irritation
   from Episkin Academy, Medtronic, TÜV SÜD
 * Discuss the challenges of toxicological risk assessments with Zimmer
   Biomet and more
 * ISO 10993-1 revision: Addressing the challenges, impact and future concerns
   with TÜV SÜD, Zimmer Biomet and the convenor of ISO TC121/SC3/WG13


GLOBAL BIOCOMPATIBILITY CHALLENGES ADDRESSED

 * NMPA keynote: Biocompatibility testing in China
 * Panel discussion: Understand the interpretations of ISO 10993 standards in
   Asia-Pacific and how to address the challenges

See The Biocompatibility Agenda


BENCHMARK BIOCOMPATIBILITY BEST PRACTICES WITH TC/194 WORKING GROUP MEMBERS AND
INDUSTRY EXPERTS INCLUDING


RON BROWN

OWNER AND PRINICIPAL TOXICOLOGIST

RISK SCIENCE CONSORTIUM, LLC


KELLY COLEMAN, PH.D., DABT, ERT, RAC

DISTINGUISHED TOXICOLOGIST, TECHNICAL FELLOW, BAKKEN FELLOW

MEDTRONIC


CHENGHU LIU

SENIOR FELLOW, DIRECTOR OF BIOLOGICAL EVALUATION DEPARTMENT

NMPA-JINAN QUALITY SUPERVISION AND INSPECTION CENTER FOR MEDICAL DEVICES


THOR ROLLINS

DIRECTOR, TOXICOLOGY AND E&L CONSULTING

NELSON LABORATORIES

Meet The Biocompatibility Speakers

Christopher Parker

Associate Department Head, In-Vivo Biocompatibility

Toxikon

"Content very good and well organised conference that suited all attendees."

Piet Christiaens

Scientific Director

Nelson Labs

"Good event with interaction from the audience."

Mollie J. Holter

Consultant & Owner

MicroBio Consulting, LLC

“As a speaker new to the event, I found this a high quality conference with the
right audience. The attendees were well educated asking good questions and
demonstrated a good baseline knowledge of biocompatibility.”

Anja Friedrich

Head of Sales Medical Device, Eurofins Medical Device Testing,

Eurofins, BioPharma Product Testing Munich GmbH

Really good event, technical and high level and very good organisation.

Ashleigh Ace

Commercial Director

Bibra toxicology

“We really enjoyed the MedTech Summit conference. Well done on achieving such
success on the virtual event!”

Christopher Parker

Associate Department Head, In-Vivo Biocompatibility

Toxikon

"Content very good and well organised conference that suited all attendees."

Piet Christiaens

Scientific Director

Nelson Labs

"Good event with interaction from the audience."

Mollie J. Holter

Consultant & Owner

MicroBio Consulting, LLC

“As a speaker new to the event, I found this a high quality conference with the
right audience. The attendees were well educated asking good questions and
demonstrated a good baseline knowledge of biocompatibility.”

Anja Friedrich

Head of Sales Medical Device, Eurofins Medical Device Testing,

Eurofins, BioPharma Product Testing Munich GmbH

Really good event, technical and high level and very good organisation.

Ashleigh Ace

Commercial Director

Bibra toxicology

“We really enjoyed the MedTech Summit conference. Well done on achieving such
success on the virtual event!”

Christopher Parker

Associate Department Head, In-Vivo Biocompatibility

Toxikon

"Content very good and well organised conference that suited all attendees."

Piet Christiaens

Scientific Director

Nelson Labs

"Good event with interaction from the audience."

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ELSEWHERE AT MEDTECH SUMMIT




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